Showing posts with label Coenzymes. Show all posts
Showing posts with label Coenzymes. Show all posts

Wednesday, October 12, 2011

What Do I Know?

So today I ponder. What would my children's life be like if I had no hope? What would it be like if I believed all of the websites, doctors and research that said my children will always be like they were and will never recover? I shudder to think about that but sometimes I see something that makes me think about just that very concept.

Today, in my Internet search for something else I happened upon the show "The Talk" and I wanted to see if Holly Robinson Peete was still one of the hosts, and unfortunately she's no longer on there because she was a great voice for Autism Awareness. Anyways going off track. So I end up on this quest to find out what some deem autism to be and what they think the prognosis is.

So I go to the HollyRod website first (because she fueled my journey for today) and I click on the Autism tab, and this is the definition that is given: "Autism is a lifelong, complex neurobiologial disorder for which there is currently no documented cure. It crosses a spectrum that ranges from relatively mild difficulties to extreme conditions involving severe language delay; repetitive and/or anti-social behavior, and even aggressive and/or self-injurious behavior. Symptoms of autism change across the life course. An autism diagnosis involves deficits in three core areas: social interaction, use of language, and behavior and interests. Researchers are scrambling to determine whether autism is linked to genetics, environment factors or a combination of both."

Next I go to Autism Speaks and their definition is: "Autism is a general term used to describe a group of complex developmental brain disorders known as Pervasive Developmental Disorders(PDD). The other pervasive developmental disorders are PDD-NOS (Pervasive Developmental Disorder- Not Otherwise Specified), Asperger Syndrome, Rett Syndrome, Rett Syndrome and Childhood Disintegrative Disorder. Many parents and professionals refer to this group as Autism Spectrum Disorders."

Finally, I went to the Autism Society of America and their definition is: "Autism is a complex developmental disability that typically appears during the first three years of life and affects a person's ability to communicate and interact with others. Autism is defined by a certain set of behaviors and is a "spectrum disorder" that affects individuals differently and to varying degrees. There is no known single cause for autism, but increased awareness and funding can help families today."

Now in saying all of that I say this, in a round about way they all give the same definition for autism, and they all really won't comment on what they think the causes are and they all say that there is no "known" cure. Now in saying that when you go onto each website and read further they do say that that there are treatments that will make life easier and that often times no one treatment will help that some children will require multiple treatments.

Both ASA and Autism Speaks give great information about the different types of treatments, biomedical and otherwise. Autism Speaks specifically gives out a great packet of information called The 100 Day Kit, and it helps parents navigate the first 100 days after the initial diagnosis. The HollyRod Foundation mainly offer support and assistance in the Greater Los Angeles area.

All of the above are great resources if you are just starting out on your Autism Journey, if you have been in the game for any length of time then the above sites will just frustrate you because it is often things that you have already know. But they are great starting points. At some point in your journey you're going to have to go behind, speech, occupational, and physical therapy. At some point you're going to have to push the envelope beyond what you feel comfortable with and do treatments that don't fit into the box of conventional medicine. That's if you want to do what the medical community considers impossible.....recover. Our kids can be recovered, it will get better if you don't give up hope.

Wishing you Blessing and Recovery,

The Fuller's

Saturday, October 1, 2011

October 1, 2011

Woke Jai Lynn up to take NADH pill and she had lots of mucus coming out of her right eye (sorry she wiped It out before I could grab my camera) then she began whining about her nose having "boogers" and wanting them out. Tried to have her blow her nose but no boogers, she continued whining so since its Saturday I just closed her door and let her rest more.

Marcus,Jr is in great spirits this morning. Took his NADH with minimal resistance, and has been hopping and signing every since.

Check out my YouTube for the fun for the day.

At approximately 3:30 pm Marcus Jr had a seizure as we were driving to the grocery store. He urinated on himself and fell asleep in the backseat of the van.

I was able to get some video of the end and after, also got some pictures so be sure to check my YouTube page out for that.

He also had/has very bad gas so it looks like another clay bath is in order. Sometimes gas is like a "prequel" to a seizure, obviously his system is fighting something.

After we got home he went right to my bed and he laid down for about two hours, ate about three helpings of dinner plus an apple then asked to watch his show. After all of the excitement he seems to be pretty calm and just chill. Not sure if this is just that this seizure has taken it out of him or we're seeing some changes in behavior. Although, I think its the first I can always hope for the second.

Jai Lynn seems to be having a difficult time today processing information (maybe it's everyday and now because I'm journaling it, it just seems like its worse. I don't know .


*One Hour time elapse*

As I was writing the above portion at about 8:30 pm my son had another seizure lasting for 25 seconds. With a recovery time of under 5 minutes. Which is big. My husband says it looks like his seizure recovery times are getting smaller and the seizures aren't lasting as long. He will be receiving a clay bath tomorrow. Tonight before bed I made sure he had his zeolyte. It seems as if he was right back to normal after this episode as he fully participated in story time (sorry no video I was making bottles) and stayed clear of his room until his bed was made.

Jai Lynn had a great day overall, she also took her zeolyte before bed and she did well during story time (received all story time reports from my husband). She was very low key today but did a lot of question asking, and a lot of conversation initiation (well at least her version of it which is asking the same question over and over again whenever she sees or hears something that reminds her of a topic of interest today it was Halloween). She was very interested about what I was doing in the kitchen (but that has been one of her big interests as of late) and she was very helpful and understanding when Marcus, Jr was having his seizures. An overall big girl. She also told me today that she is going to be a veterinarian when she grows up.

So that was our day in a nutshell, will most likely have more video tomorrow of both kids will try to post what their academic work looks now also.

Until next time,

Wishing you Blessings and Recovery

The Fullers


Friday, September 30, 2011

Day 1 9.30.11

So this I have finally switched my blog from WordPress to Blogger, the interface is much more user friendly and Blogger allows me much more blogger freedoms.

So today was day 2 on the NADH as a part of our protocol, and this morning when Marcus Jr got up all seemed well. But as I was making breakfast I hadn't heard from him and went into his room to discover that he had had a seizure. So I instantly knew that he was staying home from school because there was obviously some detoxing that he needed to do.

Once I got him back home (we had to drop his sister off at school) made him some breakfast and then gave him a clay bath. He sat in the clay bath for about 30 minutes and came out as "right as rain."

After that time he did well no more seizure episodes but I am gathering that I will have to give him more clay baths during this time of change.

Will follow up with more info and video of the kids because I need a visual, to see where my children have been and where they are going. Will also pull my resources from my old blog as well as I will be scanning and uploading what the protocol is that we are on.

Wishing you and your family wellness and recovery,

The Fuller's